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Polycomb response elements mediate the formation of chromosome higher-order structures in the bithorax complex Chiara Lanzuolo, Virginie Roure, Job Dekker, Frédéric Bantignies, and Valerio Orlando
Epigenetics Heritable changes in gene expression caused by mechanisms other than changes in the underlying DNA sequence. Chromatin remodeling via DNA or histone modification.  Heterochromatin and euchromatin Higher order chromosome structures
Techniques used FISH Chromosome Conformation Capture RNAi
Terms & Concepts Polycomb Group Genes (PcG):  Gene products are proteins that can remodel chromatin such that transcription factors cannot bind to promoter sequences in DNA (repression). PcGs play a role in silencing HOX genes through modulation of chromatin structure (i.e.  trans -acting).  Polycomb Response Elements (PRE):  Chromosomal (DNA) regulatory elements that recruit PcG factors to chromatin in vivo (i.e.  cis -acting), and  mediate epigenetic inheritance of silent and active states throughout development.  Located within the Bithorax Complex.  Bithorax Complex (BX-C):  340kb region which specifies the identities of several posterior abdominal segments; contains 3 Hox genes observed in this paper, each with corresponding PREs. HOX Genes: specify the anterior-posterior axis and segment identity during early development of  Drosophila  and other metazoans. Gene products are transcription factors which must be present in specific gradients throughout the embryo to facilitate proper development.
Hox Gene Mutant
Hox genes & PREs in BX-C Hox Genes: abd-A abd-B   Ubx PREs Fab-7 Mcp bxd  Bx
Cell Lines Cultured embryonic cell lines were used Schneider 2 (S2):  Ubx, abdB, abdA  all repressed. Schneider 3 (S3): all three  abdB  transcripts abundant,  Ubx  and  abdA  also repressed.
FISH Results
FISH Results
3C Results
3C Results-RNAi PcG protein  Polycomb  ( Pc ) synthesis was reduced via dsRNA in S2 cultures. Transcript was reduced 80% After analysis the cell line was allowed to recover  Pc  activity over ~20 cell divisions.
3C Results-RNAi
3C: Distal PREs
Hox Transcripts via rt-PCR
PRE Transcripts via rt-PCR
3C Results: S3 cells
3C Results: S3 cells
FISH: S3 cells
Conclusions Silenced BX-C assumes a highly complex topology of the locus that involves all major PcG- regulated DNA elements, including PREs and promoter interactions, as well as long distance PRE-PRE interactions.  Active BX-C domains lose contact with the core of the repressed structure. Forced reactivation of BX-C genes only affects interactions between the  AbdB, abdA,  and  Ubx  promoters and the PREs relatively distal from them. The proximal PRE-promoter higher level interaction may lead to successful re-repression when normal amounts of  Pc  are restored.
Conclusion

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Polycomb Response Elements

  • 1. Polycomb response elements mediate the formation of chromosome higher-order structures in the bithorax complex Chiara Lanzuolo, Virginie Roure, Job Dekker, Frédéric Bantignies, and Valerio Orlando
  • 2. Epigenetics Heritable changes in gene expression caused by mechanisms other than changes in the underlying DNA sequence. Chromatin remodeling via DNA or histone modification. Heterochromatin and euchromatin Higher order chromosome structures
  • 3. Techniques used FISH Chromosome Conformation Capture RNAi
  • 4. Terms & Concepts Polycomb Group Genes (PcG): Gene products are proteins that can remodel chromatin such that transcription factors cannot bind to promoter sequences in DNA (repression). PcGs play a role in silencing HOX genes through modulation of chromatin structure (i.e. trans -acting). Polycomb Response Elements (PRE): Chromosomal (DNA) regulatory elements that recruit PcG factors to chromatin in vivo (i.e. cis -acting), and mediate epigenetic inheritance of silent and active states throughout development. Located within the Bithorax Complex. Bithorax Complex (BX-C): 340kb region which specifies the identities of several posterior abdominal segments; contains 3 Hox genes observed in this paper, each with corresponding PREs. HOX Genes: specify the anterior-posterior axis and segment identity during early development of Drosophila and other metazoans. Gene products are transcription factors which must be present in specific gradients throughout the embryo to facilitate proper development.
  • 6. Hox genes & PREs in BX-C Hox Genes: abd-A abd-B Ubx PREs Fab-7 Mcp bxd Bx
  • 7. Cell Lines Cultured embryonic cell lines were used Schneider 2 (S2): Ubx, abdB, abdA all repressed. Schneider 3 (S3): all three abdB transcripts abundant, Ubx and abdA also repressed.
  • 11. 3C Results-RNAi PcG protein Polycomb ( Pc ) synthesis was reduced via dsRNA in S2 cultures. Transcript was reduced 80% After analysis the cell line was allowed to recover Pc activity over ~20 cell divisions.
  • 16. 3C Results: S3 cells
  • 17. 3C Results: S3 cells
  • 19. Conclusions Silenced BX-C assumes a highly complex topology of the locus that involves all major PcG- regulated DNA elements, including PREs and promoter interactions, as well as long distance PRE-PRE interactions. Active BX-C domains lose contact with the core of the repressed structure. Forced reactivation of BX-C genes only affects interactions between the AbdB, abdA, and Ubx promoters and the PREs relatively distal from them. The proximal PRE-promoter higher level interaction may lead to successful re-repression when normal amounts of Pc are restored.